Atlas FDA

VZV TEST

FDA 510(k) clearance K875358 · decided 1988-03-31

Clearance details

K-number
K875358
Device name
VZV TEST
Applicant
Gull Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1987-12-31
Decision date
1988-03-31
Days to decision
91 days
Clearance type
Traditional
Product code
GQX
Device class
2
Regulation number
866.3900
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Salt Lake City, UT, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VARICELLA-ZOSTER VIRUS DIRECT IMMUNOFLUORESCENCE ASSAY (K951799)Light Diagnostics1996-03-20
VZV IGM TEST (K911301)Gull Laboratories, Inc.1991-07-17
VIRGO(R) VZV-IGG ELISA (K883427)Electro-Nucleonics, Inc.1989-03-10
ENZYGNOST ANTI-VZV IGG TEST (K863317)Behring Diagnostics, Inc.1987-04-22
FIAX TEST KIT FOR VARICELLA ANTIBODY SEROLOGY (K853540)Idt, A Division of Whittaker M.A. Bioproducts1986-02-04
VARICELLA-ZOSTER-COMPLE FIX ANTIGEN AND NEG CONTRO (K852930)Microbix Biosystems, Inc.1985-11-12
GLB VARICELLA-ZOSTER VIRUS FLUORESCENT (K842096)Great Lakes Bioscience1985-01-07
ORTHO VARICELLA-ZOSTER VIRUS IDENT. (K841526)Ortho Diagnostic Systems, Inc.1984-06-25
VARICELLA-ZOSTER FA LABELLED (8-321 RF) (K770806)Flow Laboratories, Inc.1977-05-20
VARICELLA-ZOSTER FA LABELED PRESERUM (K770810)Flow Laboratories, Inc.1977-05-20

Recalls involving this device

No recalls on record reference this clearance.